A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5508628



Internal ID285315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102876000..102882368hg38UCSC Ensembl
chr10:104635757..104642125hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg386369
hg196369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17039965
Samples
Known GenesAS3MT, C10orf32-ASMT
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5508628
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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